New sperm prep device could boost IVF success
NCT ID NCT06990841
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study compares a new sperm separation device (LensHooke CA0) with the standard gradient/swim-up method to see which reduces DNA damage in sperm. Each semen sample is split, and half the partner's eggs are fertilized with sperm from each method. Researchers will check DNA fragmentation, sperm quality, embryo development, and pregnancy rates in 50 couples.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- sperm separation device (LensHooke CA0)
- What this could lead to
- If one method clearly reduces DNA damage, it could lead to better embryo quality and higher pregnancy rates in IVF.
- What could go wrong
- This is a small, early-stage study (50 participants) comparing two lab techniques, not a treatment. Results may not apply to all fertility cases.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2025
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 34 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Samples with ≥15 M/mL spermatozoa concentration * Female partner between 18 and 34 years old. * Minimum of 4 fertilized eggs in gradient/swim prep group and 4 fertilized eggs in the Lenshooke prep group for each patient Exclusion Criteria: * Samples with \<15 M/mL spermatozoa concentration * female partner \>35 years old * female patient with recurrent pregnancy loss * female patient with diminished ovarian reserve
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Get notified about this study
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Prisma Health-Upstate Fertility Center of the Caroliinas
RECRUITINGGreenville, South Carolina, 29605, United States
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